BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    AMO ARTHOSCOPES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111062·INSTRUMENT CASE MEDIUM ALUMINUM

    Flex Robotic System and Flex Colorectal Drive

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MODIFIED OSCOR PY PACING LEADS

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    MINILINK TRANSMITTER

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·February 14, 2013

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2014

    PINNACLE MTL INS NEUT36IDX50OD

    FDA Adverse Event
    Injury ·DEPUY INTL LTD·Product code KWA·January 7, 2011

    COMP RVS TRAY +5MM CO 44MM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWS·November 27, 2019

    ARCOM XL 44-36 STD HMRL BRNG

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·November 27, 2019

    Medtronic INTREPID Spinal System Coverplate, size: Small, Part Number: REF 7961330; medium, REF 7962330; large, REF 7963330; STERILE R. The INTREPID Spinal System is indicated for use with autogenous bone graft in patients with degenerative disc disease.

    FDA Recall
    Terminated ·Medtronic Sofamor Danek USA Inc·Product code MAX·February 6, 2009